Canonical Allele Identifier: PA1139702632
Gene: CDH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 967706
ClinVar RCV Id: RCV001242685
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004351.1:p.Ser111Pro
CA396457406
NM_004360.5:c.331T>C